Canonical Allele Identifier: CA2015347076

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116081A= , CM000674.2:g.9116081A= GRCh38
NC_000012.11:g.9268677A= , CM000674.1:g.9268677A= GRCh37
NC_000012.10:g.9159944A= NCBI36
NG_011717.1:g.4882T=
NG_011717.2:g.4882T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-232T= (A2M) ENSP00000323929.7:n.-232T=
ENST00000404455.2:c.-18+47T= (A2M) ENSP00000385710.2:n.-18+47T=
NM_000014.5:c.-232T= (A2M) NP_000005.2:n.-232T=
NM_001347423.1:c.-18+47T= (A2M) NP_001334352.1:n.-18+47T=
NM_001347424.1:c.-685T= (A2M) NP_001334353.1:n.-685T=
NM_001347425.1:c.-522T= (A2M) NP_001334354.1:n.-522T=
XM_017018683.1:c.*34-9293A= (KLRG1) XP_016874172.1:n.*34-9293A=
XM_017018684.1:c.*34-19005A= (KLRG1) XP_016874173.1:n.*34-19005A=
XM_017018685.1:c.*33+57915A= (KLRG1) XP_016874174.1:n.*33+57915A=
NM_001347423.2:c.-18+47T= (A2M) NP_001334352.2:n.-18+47T=